Synthetic Route of 5908-62-3, Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 5908-62-3, molcular formula is C3H7NO2S, introducing its new discovery.
Penultimate group effects in free radical telomerizations of acrylamides
The telomerization of several acrylamides, most containing chiral auxiliary groups, was investigated. The first-formed stereogenic center in the n = 2 telomer (the penultimate center) has a significant effect on the configuration of the second (ultimate) center in the product. The penultimate chiral center of oxazolidine-derived acrylamides directs the configuration of the ultimate center such that the erythro n = 2 product is preferred. Sultam-substituted acrylamides preferentially lead, on the other hand, to threo products or give products with little stereoselectivity.
If you¡¯re interested in learning more about Electric Literature of 1111-67-7, below is a message from the blog Manager. Synthetic Route of 5908-62-3
Reference£º
Quinuclidine – Wikipedia,
Quinuclidine | C7H582N | ChemSpider